IL230257A - Penta/hexamethyl-3,4,5,8-tetrahydro -1(2h)-naphthalenone derivatives with aromatic notes - Google Patents

Description

PENTA/HEXAMETHYL -3, 4, 5, 8- TETRAHYDRO - 1 ( 2H) - NAPHTHALENONE DERIVATIVES WITH AROMATIC NOTES Technical field The present invention relates to the field of perfumery. More particularly, it 5 concerns some penta/hexamethyl-3,4,5,8-tetrahydro-l(2H)-naphthalenone derivatives of formula (I), as defined below, which are useful perfuming ingredients. The present invention comprises also the invention’s compounds as part of a perfuming composition or of a perfuming consumer product. to Prior art To the best of our knowledge, the invention’s compounds of formula (I) are novel. To the best of our knowledge, the closest analogues known in the perfumery and belonging to the same broad olfactive family are the ones described in EP 1689728, which have anyway a different stmcture and also a significantly different musk odor type. 15 These prior art documents do not report or suggest any organoleptic properties of the compounds of formula (I), as discussed futher below, and do not report or suggest any use of said compounds in the field of perfumery.

Description of the invention 20 We have now surprisingly discovered that a compound of formula wherein the dotted line represents a carbon-carbon single or double bond and R 25 represents a hydrogen atom or a methyl group; can be used as perfuming ingredient, for instance to impart odor notes of the muskyearthy and woody, aromatic-fresh character.

For the sake of clarity, by the expression “wherein one dotted line represents a carbon-carbon single or double bond”, or the similar, it is meant the normal meaning understood by a person skilled in the art, i.e. that the whole bonding (solid and dotted line) between the carbon atoms connected by said dotted line is a carbon-carbon single or double bond.

According to an embodiment of the invention, said R represents a methyl group. According to any one of the above embodiments of the invention, when said dotted line represents a carbon-carbon single bond, the two hydrogen atoms bonded to the carbons 4a and 8a are in a relative trans configuration.

According to any one of the above embodiments of the invention, said dotted line represents a carbon-carbon double bond.

As specific examples of the invention’s compounds, one may cite, as non-limiting example, 5,5,6,7,8,8-hexamethyl-3,4,5,8-tetrahydro-l(2Fl)-naphthalenone.

This compound possesses a musky-earthy odor characterized by a pear, woody and aromatic-chamomile-fresh character. The odor of this compound has a surprising musky and fresh combination reminding surprisingly of a mix of the earthy aspect of the well known musk Tonalide (5,6,7,8-tetrahydro-3,5,5,6,8,8-hexamethyl-2-naphthyl)-1-ethanone; origin: PFW, Flolland) and of the fruity/fresh aspect of Flelvetolide® ((1S,1'R)-2-[l-(3',3'-dimethyl-r-cyclohexyl)ethoxy]-2-methylpropyl propanoate; origin: Firmenich SA, Switzerland). When the organoleptic properties of this compound are compared to those of the prior art (6RS,7RS)-5,5,6,7,8,8-hexamethyl-3,4,5,6,7,8-hexahydronaphthalen-l(2Fl)-one (described in W02005/054220), then the invention’s compound although having musk-earthy notes distinguishes itself by having a higher impact/strength, strong woody/ambrette note together with a fresh aromatic character of the chamomile type (all absent or almost absent from the prior art compound) and being devoid of significant animal connotation typical of the prior art compound. Furthermore, 5,5,6,7,8,8-hexamethyl-3,4,5,8-tetrahydro-l(2Fl)-naphthalenone surprisingly possesses odor notes which are as strong/powerful as the prior art analogue (6RS,7RS)-5,5,6,7,8,8-hexamethyl-3,4,5,6,7,8-hexahydronaphthalen-l(2Fl)-one despite the quite different conformational shape, and this is quite surprising.

As other specific, but non- limiting, examples of the invention’s compounds, one may cite the following ones in Table 1: Table 1 : Invention’ s compounds and their odor properties According to a particular embodiment of the invention, the compounds of formula (I) are 5,5,6,7,8,8-hexamethyl-3,4,5,8-tetrahydro-l(2H)-naphthalenone, 5,5,6,7,8,8-hexamethyl-3,4,4aoc,5,8,8a -hexahydro-l(2H)-naphthalenone or 5, 5, 6,8,8-pentamethyl-3 ,4,5,8-tetrahydro- 1 (2H)-naphthalenone.

When the odor of the invention’s compounds is compared with that of the prior art, then the invention’s compounds distinguish themselves by a clearly stronger woody/ambrette-like note, by having a characteristic aromatic note (absent in the prior art compounds) and by lacking or not possessing a significant, animal notes which are characteristic of some of the prior art compounds. Said differences lend the invention’s compounds and the prior art compounds to be each suitable for different uses, i.e. to impart different organoleptic impressions.

The compounds of formula (I), to the best of our knowledge, are also new compounds, and therefore another object of the present invention.

As mentioned above, the invention concerns the use of a compound of formula (I) as perfuming ingredient. In other words, it concerns a method to confer, enhance, improve or modify the odor properties of a perfuming composition or of a perfumed article, which method comprises adding to said composition or article an effective amount of at least a compound of formula (I). By “use of a compound of formula (I)” it has to be understood here also the use of any composition containing a compound (I) and which can be advantageously employed in perfumery industry.

Said compositions, which in fact can be advantageously employed as perfuming ingredients, are also an object of the present invention.

Therefore, another object of the present invention is a perfuming composition comprising: i) as perfuming ingredient, at least one invention’s compound as defined above; ii) at least one ingredient selected from the group consisting of a perfumery carrier and a perfumery base; and iii) optionally at least one perfumery adjuvant.

By “perfumery carrier” we mean here a material which is practically neutral from a perfumery point of view, i.e. that does not significantly alter the organoleptic properties of perfuming ingredients. Said carrier may be a liquid or a solid.

As liquid carrier one may cite, as non-limiting examples, an emulsifying system, i.e. a solvent and a surfactant system, or a solvent commonly used in perfumery. A detailed description of the nature and type of solvents commonly used in perfumery cannot be exhaustive. However, one can cite as non-limiting example solvents such as dipropyleneglycol, diethyl phthalate, isopropyl myristate, benzyl benzoate, 2-(2-ethoxyethoxy)- 1 -ethanol or ethyl citrate, which are the most commonly used. For the compositions which comprise both a perfumery carrier and a perfumery base, other suitable perfumery carriers than those previously specified, can be also ethanol, water/ethanol mixtures, limonene or other terpenes, isoparaffins such as those known under the trademark Isopar® (origin: Exxon Chemical) or glycol ethers and glycol ether esters such as those known under the trademark Dowanol® (origin: Dow Chemical Company).

As solid carrier one may cite, as non-limiting examples, absorbing gums or polymers, or yet encapsulating materials. Examples of such materials may comprise wall forming and plasticizing materials, such as mono, di- or trisaccharides, natural or modified starches, hydrocolloids, cellulose derivatives, polyvinyl acetates, polyvinylalcohols, proteins or pectins, or yet the materials cited in reference texts such as H. Scherz, Hydrokolloids : Stabilisatoren, Dickungs- und Gehermittel in Lebensmittel, Band 2 der Schriftenreihe Lebensmittelchemie, Lebensmittelqualitat, Behr's VerlagGmbH & Co., Hamburg, 1996. The encapsulation is a well known process to a person skilled in the art, and may be performed, for instance, using techniques such as spray-drying, agglomeration or yet extrusion ; or consists of a coating encapsulation, including coacervation and complex coacervation techniques.

By “perfumery base” we mean here a composition comprising at least one perfuming co-ingredient.

Said perfuming co-ingredient is not of formula (I). Moreover, by “perfuming co ingredient” it is meant here a compound, which is used in a perfuming preparation or a composition to impart a hedonic effect. In other words such a co-ingredient, to be considered as being a perfuming one, must be recognized by a person skilled in the art as being able to impart or modify in a positive or pleasant way the odor of a composition, and not just as having an odor.

The nature and type of the perfuming co-ingredients present in the base do not warrant a more detailed description here, which in any case would not be exhaustive, the skilled person being able to select them on the basis of his general knowledge and according to intended use or application and the desired organoleptic effect. In general terms, these perfuming co-ingredients belong to chemical classes as varied as alcohols, lactones, aldehydes, ketones, esters, ethers, acetates, nitriles, terpenoids, nitrogenous or sulphurous heterocyclic compounds and essential oils, and said perfuming co-ingredients can be of natural or synthetic origin. Many of these co-ingredients are in any case listed in reference texts such as the book by S. Arctander, Perfume and Flavor Chemicals, 1969, Montclair, New Jersey, USA, or its more recent versions, or in other works of a similar nature, as well as in the abundant patent literature in the field of perfumery. It is also understood that said co-ingredients may also be compounds known to release in a controlled manner various types of perfuming compounds.

By “perfumery adjuvant” we mean here an ingredient capable of imparting additional added benefit such as a color, a particular light resistance, chemical stability, etc. A detailed description of the nature and type of adjuvant commonly used in perfuming bases cannot be exhaustive, but it has to be mentioned that said ingredients are well known to a person skilled in the art.

An invention’s composition consisting of at least one compound of formula (I) and at least one perfumery carrier represents a particular embodiment of the invention as well as a perfuming composition comprising at least one compound of formula (I), at least one perfumery carrier, at least one perfumery base, and optionally at least one perfumery adjuvant.

It is useful to mention here that the possibility to have, in the compositions mentioned above, more than one compound of formula (I) is important as it enables the perfumer to prepare accords, perfumes, possessing the odor tonality of various compounds of the invention, creating thus new tools for his work.

For the sake of clarity, it is also understood that any mixture resulting directly from a chemical synthesis, e.g. a reaction medium without an adequate purification, in which the compound of the invention would be involved as a starting, intermediate or end-product could not be considered as a perfuming composition according to the invention as far as said mixture does not provide the inventive compound in a suitable form for perfumery.

Furthermore, the invention’s compound can also be advantageously used in all the fields of modem perfumery, i.e. fine or functional perfumery, to positively impart or modify the odor of a consumer product into which said compound (I) is added. Consequently, a perfuming consumer product which comprises: i) as perfuming ingredient, at least one compound of formula (I), as defined above; and ii) a perfumery consumer base; is also an object of the present invention.

The invention’s compound can be added as such or as part of an invention’s perfuming composition.

For the sake of clarity, it has to be mentioned that, by “perfuming consumer product” it is meant a consumer product which is expected to deliver at least a perfuming effect, in other words it is a perfumed consumer product. For the sake of clarity, it has to be mentioned that, by “perfumery consumer base” we mean here the functional formulation, as well as optionally additional benefit agents, corresponding to a consumer product which is compatible with perfuming ingredients and is expected to deliver a pleasant odor to the surface to which it is applied (e.g. skin, hair, textile, or home surface). In other words, a perfuming consumer product according to the invention comprises the functional formulation, as well as optionally additional benefit agents, corresponding to the desired consumer product, e.g. a detergent or an air freshener, and an olfactive effective amount of at least one invention’ s compound.

The nature and type of the constituents of the perfumery consumer base do not warrant a more detailed description here, which in any case would not be exhaustive, the skilled person being able to select them on the basis of his general knowledge and according to the nature and the desired effect of said product.

Non-limiting examples of suitable perfumery consumer base can be a perfume, such as a fine perfume, a cologne or an after-shave lotion; a fabric care product, such as a liquid or solid detergent, a fabric softener, a fabric refresher, an ironing water, a paper, or a bleach; a body-care product, such as a hair care product (e.g. a shampoo, a coloring preparation or a hair spray), a cosmetic preparation (e.g. a vanishing cream or a deodorant or antiperspirant), or a skin-care product (e.g. a perfumed soap, shower or bath mousse, oil or gel, or a hygiene product); an air care product, such as an air freshener or a “ready to use” powdered air freshener; or a home care product, such as a wipe, a dish detergent or hard- surface detergent.

Some of the above-mentioned consumer product bases may represent an aggressive medium for the invention’s compound, so that it may be necessary to protect the latter from premature decomposition, for example by encapsulation or by chemically bounding it to another chemical which is suitable to release the invention’s ingredient upon a suitable external stimulus, such as an enzyme, light, heat or a change of pH.

The proportions in which the compounds according to the invention can be incorporated into the various aforementioned articles or compositions vary within a wide range of values. These values are dependent on the nature of the article to be perfumed and on the desired organoleptic effect as well as the nature of the co-ingredients in a given base when the compounds according to the invention are mixed with perfuming co ingredients, solvents or additives commonly used in the art.

For example, in the case of perfuming compositions, typical concentrations are in the order of 0.001 % to 45 % by weight, or even more, of the compounds of the invention based on the weight of the composition into which they are incorporated. Concentrations lower than these, such as in the order of 0.1 % to 20% by weight, can be used when these compounds are incorporated into perfumed articles, percentage being relative to the weight of the article.

The invention’s compounds can be prepared according to a method as described in the Examples herein below.

Examples The invention will now be described in further detail by way of the following examples, wherein the abbreviations have the usual meaning in the art, the temperatures are indicated in degrees centigrade (°C) ; the NMR spectral data were recorded in CDCI3 (if not stated otherwise) with a 360 or 400 MHz machine for 111 and 13C, the chemical shifts d are indicated in ppm with respect to TMS as standard, the coupling constants J are expressed in Hz.

Example 1 Synthesis of compounds of formula (I) methyl 2,3,3,6,6-pentamethyl-4-oxocyclohex-l-enecarboxylate (2a) A solution of tBuOK (16.28 g in 70 ml diglyme) and Mel (11.32 ml) were added simultaneously over 1.5h to a solution of methyl 2,6,6-trimethyl-4-oxocyclohex-2-enecarboxylate (15g, 72.7 mmol) in diglyme (80ml) cooled at 0°C. The mixture was stirred at 0°C for 2 hours and then quenched with HC1 5%. The mixture was extracted with Ft2() and the organic layer was washed with water, saturated NH4OH solution, water, saturated bicarbonate solution, and brine. The collected organic layers were dried with MgSC>4 and the solvents were evaporated. The crude was purified by distillation (125°C, 0.1 mbar) and column chromatography (Silicagel, cyclohexane/EtOAc 98/2) to give (2a). Yield: 27%. methyl 2,3,3,5,6,6-hexamethyl-4-oxocyclohex-l-enecarboxylate (2b) A solution of (2a) (l.Og, 4.38 mmol) in THF (5 ml) was slowly added to a solution of LDA (freshly prepared from 3.13 ml BuLi 1.54M and 0.71 ml of iPr2NH) in THF (5 ml). The solution was stirred at -78°C for 30 min and then a Mel (0.41 ml) was added. The mixture was stirred at -78°C for 30 minutes then slowly warmed at room temperature After 1 hour a saturated solution of NH4C1 was added and the mixture was extracted with pentane. The organic layer was washed with saturated NH4C1 solution, bicarbonate, and brine. The collected organic layers were dried with MgSC>4 and concentrated to dryness. The cmde was purified by column chromatography (silicagel, cyclohexane/EtOAc 98/2). Yield 78%. methyl 4-hydroxy-2,3,3,4,6,6-hexamethylcyclohex-l-enecarboxylate (3a) A solution of CeC¾ (1.51 equiv.) in THF (75 ml) was stirred at room temp for 1 hour. The suspension was cooled down to -78°C, MeLi (1.50 equiv., 1.46M in Et20) was slowly added over 10 minutes, followed by the addition of a solution of (2a) (20.31 mmol) in THF (15 ml). After 30 minutes, the mixture was allowed to warm to 0°C and quenched by adding NH4C1 and ice. The mixture was extracted with Et20 and the organic layers were washed with water, saturated bicarbonate solution, and brine. After drying with MgS04, the solution was concentrated and distilled (125°C, 0.1 mbar). Yield 99%. methyl 4-hydroxy-2,3,3,4,5,6,6-heptamethylcyclohex-l-enecarboxylate (3a) As described above for (3a) provided it used (2b) as starting material. Yield 93%. methyl 2,3,3,4,6,6-hexymethylcyclohexa-J4-dienecarboxylate (4a) Compound (3a) (30 mmol) and pTSA (10 w/w%) were dissolved in cyclohexane (90ml). The mixture was refluxed in a Dean-Stark apparatus for 2 hours. The mixture was cooled at room temperature and a 5% NaOH solution was added. The mixture was extracted with Et20 and the organic layer was washed with a saturated bicarbonate solution and brine. The collected organic layers were dried with MgS04 and concentrated. The residue was purified by column chromatography (silicagel, cyclohexane/EtOAc 91/9). Yield: 90%. methyl 2,3,3,4,5,6,6-heptamethylcyclohexa-J4-dienecarboxylate (4b) As described above for (4a) provided it used (3b) as starting material. Yield: 67%.

(E)-(l-(2,2,4,5,5-pentamethyl-6-methylenecyclohex-3-enylidene)allyloxy) trimethylsilane (5a) A 1.35M solution of nBuLi in hexane (5.85 mmol) was added dropwise to a solution of (4a) (4.50 mmol) in THF (10 ml) cooled at -10°C. When the addition was completed, the cooling bath was removed and the yellow mixture was stirred for 15 min at room temperature. A solution of vinyl magnesium bromide (1M in THF, 5.85 mmol) was added and the mixture was stirred at 35 °C for 30 minutes. The solution was then cooled to -20°C, TMSC1 (13.5 mmol) was added within 5 min, and then the solution was stirred at room temp for 50 minutes. After evaporation of the solvents the product was isolated by bulb-to-bulb distillation (130°C, 0.04 mbar) to give a colorless oil. Yield: 73%.

(E)-(l-(2,2,3,4,5,5-hexamethyl-6-methylenecyclohex-3-enylidene)allyloxy) trimethylsilane (5b) As described above for (5a) provided it used (4b) as starting material. Yield: 75%. 5.5.6. 8.8-Pentamethyl-3,4, 5, 8-tetrahydro-l ( 2H)-naphthalenone (6a) A solution containing (5a) (2.5 mmol) in toluene (15 ml) was injected over 1 hour through a 20 cm column packed with quartz tubes heated at 410°C using argon as carrier. The column was washed with 5 ml of pure toluene and the collected mixture was evaporated to dryness. The concentrate was added to a solution of oxalic acid (1.12 mmol) in THF (10 ml) and water (1 ml) and the mixture was stirred at room temperature for 1 hour then quenched with a saturated bicarbonate solution and extracted with diethylether. The organic layer was washed with water and brine, then dried with MgS04, and evaporated to dryness. The cmde was purified by bulb-to-bulb distillation and column chromatography (Silicagel, Cyclohexane/EtOAc 99/1). Yield: 62%. 13C-NMR: 19.0 (q), 23.4 (t), 25.6 (q), 26.9 (t), 28.7 (q), 34.6 (s), 40.3 (t), 40.4 (s), 132.0 (s), 134.0 (d), 136.6 (s), 160.9 (s), 199.9 (s); 5.5.6. 7.8.8-Hexamethyl-3,4, 5, 8-tetrahydro-l ( 2H)-naphthalenone (6b) As described above for (6a) provided it used (5b) as starting material. Yield: 47%. 13C-NMR: 14.7 (q), 14.9 (q), 23.4 (t), 25.7 (q), 25.8 (q), 27.2 (t), 37.6 (s), 40.6 (s), 40.9 (t), 127.1 (s), 132.7 (s), 136.7 (s), 160.3 (s), 200.0 (s). 5.5.6. 7.8.8-Hexamethyl-3,4,4a a, 5, 8, 8 a b- h exa hyd ro - / ( 2H)-naphthalenone A mixture of (6b) (1.97g, 6.03 mmol) and Pd/C (10%, 200 mg) and EtOH (20 ml) was stirred in a pressure reactor under 1¾ (80 bar) at 75°C for 7 hours. The mixture was filtered and the filtrate concentrated. The cmde was purified by column chromatography (Silicagel, pentane/Et20 99:1). Yield: 46%. 13C-NMR: 14.6 (q), 15.1 (q), 20.6 (q), 21.5 (q), 22.2 (t), 24.4 (t), 26.0 (q), 26.0 (q), 38.4 (s), 38.6 (s), 41.1 (t), 43.7 (d), 57.1 (d), 132.6 (s), 133.4 (s), 215.0 (s).

Example 2 Preparation of a perfuming composition A perfuming composition for shower gel was prepared by admixing the following ingredients: Parts by weight Ingredient 150 Benzyl acetate 20 Geranyl acetate 10 Aldehyde C 11 lie 400 Hexylcinnamic Aldehyde 20 Ambrox® 11 20 Gamma undecalactone 20 Methyl benzoate 150 Citronellol 100 Coumarine 100 Cyclosal 10 10%* Damascenone 30 Estragole 1200 Florol® 2) 400 Hedione® 3) HC 100 1 , 3 -B enzodioxole- 5 -carb aldehyde 250 ISO E® 4) Super 250 Alpha iso-methyl ionone 100 Jasmin essential oil 350 Linalool 50 Crystal moss 800 Hedione® 5) 350 Phenethylol 20 Polys antol® 6) 100 Vanilline 100 Violette essential oil 200 Bergamote essential oil 200 Ylang essential oil 5500 * in dipropyleneglycol 1) (-)-(8R)-8,12-epoxy-13,14,15,16-tetranorlabdane; origin: Firmenich SA, Geneva, Switzerland 2) tetrahydro-2-isobutyl-4-methyl-4(2Fl)-pyranol; origin: Firmenich SA, Geneva, Switzerland 3) methyl cis-dihydrojasmonate; origin: Firmenich SA, Geneva, Switzerland 4) l-(octahydro-2,3,8,8-tetramethyl-2-naphtalenyl)-1-ethanone; origin: International Flavors & Fragrances, USA 5) methyl dihydrojasmonate; origin: Firmenich SA, Geneva, Switzerland 6) 3,3-dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-l-yl)-4-penten-2-ol; origin: Firmenich SA, Geneva, Switzerland The addition of 4500 parts by weight of 5,5,6,7,8,8-hexamethyl-3,4,5,8-tetrahydro-l(2Fl)-naphthalenone to the above-described composition imparted to the latter a strong musky odor and reinforced the clean fresh- aldehy die topnote. It also pushed the woody aspect of the fragrance.

When instead of the invention’s compound was used the same amount of the prior art (6RS,7RS)-5,5,6,7,8,8-hexamethyl-3,4,5,6,7,8-hexahydronaphthalen-l(2Fl)-one, the addition gave a lower degree of muskyness, which was also less clean and more earthy and animalic, and pushed the powderyness side of the composition.

Example 3 Preparation of a perfuming composition A perfuming composition for eau de toilette for men was prepared by admixing the following ingredients: Parts by weight Ingredient 100 Benzyl acetate 100 Badiane essential oil 1500 Bergamote essential oil 150 Cinnamon oil 50 Cardamome 30 Ciste essential oil 600 Coumarine 100 Ethylvanilline 400 Eugenol 50 Ginger oil 400 Hedione® u HC 10 Isobutylquinoleine 700 Lavender essential oil 1000 Linalool 400 Lyral® 2) 400 Mandarine essential oil 100 Mint essential oil 20 Crystal moss 700 Nirvanol® 3) 20 Patchouli oil 300 Santal essential oil 200 Sclary sage 500 Ylang 80 Civette 40 Pine essential oil 50 White thyme 8000 * in dipropyleneglycol 1) methyl cis-dihydrojasmonate; origin: Firmenich SA, Geneva, Switzerland 2) 4/3-(4-hydroxy-4-methylpentyl)-3-cyclohexene-1-carbaldehyde; origin: International Flavors & Fragrances, USA 3) 3,3-dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-l-yl)-4-penten-2-ol; origin: Firmenich SA, Geneva, Switzerland The addition of 2000 parts by weight of 5,5,6,7,8,8-hexamethyl-3,4,5,8-tetrahydro-l(2H)-naphthalenone to the above-described composition imparted to the latter a clean (not

Claims (7)

230257/3 Claims

1. A compound of formula wherein the dotted line represents a carbon-carbon single or double bond and R represents a hydrogen atom or a methyl group.

2. A compound according to claim 1, wherein R represents a methyl group.

3. A compound according to claim 1 or 2, wherein said dotted line represents a carbon-carbon double bond.

4. As a compound according to claim 1, 5,5,6,7,8,8-hexamethyl-3,4,5,8-tetrahydro- 1 (2H)-naphthalenone, 5 , 5 , 6 , 7 , 8 , 8 -hexamethyl- 3 , 4 ,4aa , 5 , 8 , 8 ab -he x ahydro -l(2H)-naphthalenone or 5,5,6,8,8-pentamethyl-3,4,5,8-tetrahydro-l(2H)-naphthalenone.

5. A method to confer, enhance, improve or modify the odor properties of a perfuming composition or of a perfumed article, which method comprises adding to said composition or article an effective amount of at least the compound of claim 1

6. A perfuming composition comprising i) the compound of claim 1 ; ii) at least one ingredient selected from the group consisting of a perfumery carrier and a perfumery base; and iii) optionally at least one perfumery adjuvant.

7. A perfuming consumer product comprising: i) the compound of claim 1 ; ii) a perfumery consumer base.